General Information

Job Advert Title
Real World Data Scientist
Location
United Kingdom
Function/Business Area
Research
Employment Class
Permanent

Description

Real World Data Scientist

About Astellas

Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com.

Are you driven to make a real difference in the lives of patients?

We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact.

Location and Working Environment

This position is hybrid and will require you to be onsite one days per quarter in Addlestone, Surrey UK office.

Astellas’ Responsible Flexibility Guidelines Statement - At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines.

Purpose & Scope

  • We are hiring a Real-World Data Scientist to join our Real-World Data Science (RWDS) team. As a Senior Manager of RWDS, you will be an analytic researcher informing and conducting Real World Data (RWD) studies at any time in the drug lifecycle.
  • Work directly within the RWDS team to execute observational studies for internal and external consumption and partner closely with Development, Medical Affairs, and Pharmacovigilance/ Pharmacoepidemiology colleagues in their research. Additionally, you will collaborate closely with others in RWDS, Biostatistics and the broader Quantitative Sciences & Evidence Generation department to enhance our RWD and analytics offerings.
  • RWDS is multidisciplinary and provides RWE strategic input, study design, statistical and programming support to projects. Team members apply their unique knowledge, skills and experience in teams to deliver decision-shaping real-world evidence.

Role and Responsibilities

  • Proven pharmaceutical industry hands-on experience in analyzing RWD, including major EHR and claims databases from the US, UK, EU, and/or Japan.
  • Experience in analyzing a diverse set of RWD study types (description, association, prediction, causation), including incidence & prevalence, treatment pattern, healthcare resource utilization, cost, outcomes, and effectiveness.
  • Proficiency in SQL, and SAS or R required, with working knowledge of Python beneficial.
  • Well-versed in data visualization, statistical analysis, and preferably machine learning methodologies.
  • Proficiency in planning analyses for non-interventional studies, preferably for primary data collection (i.e., prospective) as well as secondary use of data.
  • Committed to seeking innovative methodology to generate data-driven insights.

Continue: Role and Responsibilities

  • Responsible for effective planning, oversight, and execution of Clinical Development Plans and pre/post-POC trials for assigned assets and due diligence projects.
  • Ensure expert clinical operations strategy input is provided to Primary Focus Area and/or Asset Teams.
  • Develop clinical program budgets and resource estimates for assigned assets and due diligence projects.
  • Provide oversight of budget and resources during execution of clinical trials.
  • Provide oversight and guidance to extended team members in completing program deliverables according to agreed timelines and quality standards, including awareness and escalation of high impact quality-related topics for assigned programs.
  • Provide input on clinical operational matters for interactions with regulatory authorities and key opinion leaders, either globally or regionally, as applicable

Required Qualifications

  • A Doctorate or Master's Degree in Statistics, Data Science, Pharmacoepidemiology or equivalent.

What awaits you at Astellas?

  • Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide.
  • Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day.
  • Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare.
  • A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions.

Our Organizational Values and Behaviors

  • Impact
  • Innovation
  • Integrity
  • One Astellas
  • Accountability
  • Courage
  • Sense of Urgency
  • Outcome Focus

Benefits


We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help.

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